Comparing oxycodone and sufentanil for pain management after laparoscopic hysterectomy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness and safety of oxycodone versus sufentanil in patient-controlled intravenous analgesia (PCIA) for patients undergoing laparoscopic hysterectomy. Participants will be divided into two groups, with one receiving oxycodone and the other receiving sufentanil for pain management. Pain levels will be assessed at various intervals post-surgery, and the use of additional pain relief medications and any adverse effects will be monitored. The goal is to identify the most effective analgesic approach for postoperative pain management in this surgical context.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* selective laparoscopic hysterectomy
* general anesthesia
* ASA classification I - III
* aged 18 - 65 years

Exclusion Criteria:

* allergy to oxycodone or any other drugs will be used in the study
* preoperative opioids medication
* opioids abuse
* hepatic or renal dysfunction
* cardiovascular or pulmonary dysfunction
* lack of full civil capacity or refuse to participate

Where it's running

• Affiliated hospital of Nantong University
  Nantong, Jiangsu, China Recruiting

Study contacts

• Study coordinator: Siyuan Liu, PhD
• Email: tdfylsy@ntu.edu.cn
• Phone: +86-85050301

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.